ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "T Cell"

  • Abstract Number: 1762 • ACR Convergence 2023

    Single-cell RNA Sequencing Analysis and Immune Profiling of Antigen-specific T Cells in Patients with Rheumatoid Arthritis and Healthy Controls

    JING SONG1, Cliff Rims1, Matthew Dufort1, Peter Linsley1, Eddie James2 and Jane Buckner2, 1Benaroya Research Institute, Seattle, WA, 2Benaroya Research Institute at Virginia Mason, Seattle, WA

    Background/Purpose: Single-cell analysis has emerged as a powerful tool for investigating the transcriptomics and T-cell receptor (TCR) diversity in patients with rheumatoid arthritis (RA). However,…
  • Abstract Number: 0080 • ACR Convergence 2023

    Pharmacological Inhibition of PRMT5 Demonstrates Broad Efficacy in Multiple Preclinical Models of Autoimmunity and Inflammation by Suppressing Th1, Th17 and TNF-Mediated Inflammatory Responses

    Neha Bhagwat1, Kumar Penmetsa2, Matt Devalaraja3, Suzana Marusic4, Cornelia M. Weyand5, Shozo Ohtsuki6, Peggy Scherle1 and Kris Vaddi1, 1Prelude Therapeutics, Inc, Wilmington, DE, 2Thermo Fisher Scientific, Philadelphia, PA, 3Nipuna Therapeutics, Waltham, MA, 4Hooke Laboratories LLC, Lawrence, MA, 5Mayo Clinic School of Medicine and Stanford University, Rochester, MN, 6Mayo Clinic College of Medicine and Science, Stanford University School of Medicine, Rochester, MN

    Background/Purpose: Protein arginine methyltransferase 5 (PRMT5) is the major type II PRMT that catalyzes the formation of symmetrical dimethyl arginine (SDMA) on protein substrates and…
  • Abstract Number: 0303 • ACR Convergence 2023

    Development of a Human Cytotoxic Myoinjury Model with CD8+ T Cells and Muscle Cells Differentiated from Human Induced Pluripotent Stem Cells

    Hisanori Hasegawa1, Soki Kashima2, Makoto Otsu3, Hideki Taniguchi4 and Shinsuke Yasuda5, 1Department of Rheumatology, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University (TMDU) and Institute of Global Affairs, Tokyo Medical and Dental University (TMDU), Tokyo, Japan, 2Laboratory of Immunology, Institute for Life and Medical Sciences, Kyoto University and Department of Urology, Akita University Graduate School of Medicine, Akita, Japan, 3Division of Hematology, Department of Laboratory Sciences, School of Allied Health Sciences, Kitasato University, Sagamihara, Japan, 4Division of Stem Cell Processing/Stem Cell Bank, Center for Stem Cell Biology and Regenerative Medicine, The Institute of Medical Science, Tokyo, Japan, 5Department of Rheumatology, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University (TMDU), Tokyo, Japan

    Background/Purpose: CD8+ cytotoxic lymphocytes (CTLs) play a crucial role in the myoinjury of polymyositis (PM). Nonetheless, conventional treatment for PM depends on high-dose glucocorticoids with…
  • Abstract Number: 0937 • ACR Convergence 2023

    IL-4+ and IFN-α+ Profibrotic T Cells Aggravate Systemic Sclerosis via STIM1/STING Signaling in SKG Mice

    Ji Won Yang1, Kun Hee Lee2, Jin Seok Woo2, Ha Yeon Jeong2, JeongWon Choi2, Eui-Jong Kwon1, Mi-La Cho2 and Sung-Hwan Park1, 1Division of Rheumatology, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea, 2Rheumatism Research Center, Catholic Research Institute of Medical Science, College of Medicine, The Catholic University of Korea, Seoul, South Korea

    Background/Purpose: Systemic sclerosis (SS), also known as scleroderma, is a chronic autoimmune disease caused by inflammation, tissue fibrosis, and vasculopathy. Although the pathological mechanisms of…
  • Abstract Number: 1769 • ACR Convergence 2023

    TNF-Stimulated Production of IL-15 by Fibroblast-Like Synoviocytes Mediates Human Resident Memory T Cells Development in Synovial Organoid Model

    Margaret Chang1, Maryrose Hahn2, Madison Mangin1, Brian Wauford1, Rachel Blaustein3, Lauren Henderson1, Kevin Wei4 and Peter Nigrovic1, 1Boston Children's Hospital, Boston, MA, 2Division of Immunology, Boston Children's Hospital, Boston, MA, 3Brigham and Women's Hospital, Boston, MA, 4Brigham and Women's Hospital and Harvard Medical School, Boston, MA

    Background/Purpose: Rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) are chronic autoimmune diseases that tend to flare repeatedly in the same joints, displaying joint-specific memory.…
  • Abstract Number: 0081 • ACR Convergence 2023

    RA Disease Activity Influence the Frequency and Phenotype of Citrulline Reactive CD4 T Cells in DRB1*04:04 ACPA+ RA Patients

    Cliff Rims1, Anne Hocking1, Sylvia Posso1, Bernard Ng2, Jeffrey Carlin3, Jane Buckner4 and Eddie James4, 1Benaroya Research Institute, Seattle, WA, 2Veteran Affairs, Seattle, WA, 3Virginia Mason Medical Center, Seattle, WA, 4Benaroya Research Institute at Virginia Mason, Seattle, WA

    Background/Purpose: The presence of ACPA in RA signifies an immune response toward citrullinated auto-antigens in disease pathogenesis and persistence. RA is a T cell mediated…
  • Abstract Number: 0431 • ACR Convergence 2023

    Senescence and Cell Exhaustion in CD4+ and CD8+ Lymphocytes in Rheumatoid Arthritis Patients in Remission Without Treatment

    Rodolfo Jiménez-Soto1, Luis llorente2, Guadalupe Lima1, Luisa Alanis Saenz1, Amairani Gomez Rodriguez1, Hilda Marin Lopez1, Erik Cimé-Aké1 and Juan Jakez-Ocampo1, 1Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 2Departamento de Inmunología y Reumatología, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico

    Background/Purpose: T cells are important among the several risk factors and immunological markers implicated in rheumatoid arthritis (RA). The goal of this study was to…
  • Abstract Number: 1052 • ACR Convergence 2023

    Unique Cellular and Autoantibody Signatures in Patients with irAEs Revealed by Longitudinal Immune Tracking

    Sokratis Apostolidis1, Kyra Sacksith1, Bria Fulmer1, Zoe Quandt2, Mark Anderson2, Terri Laufer3 and E. John Wherry1, 1University of Pennsylvania, Philadelphia, PA, 2University of California San Francisco, San Franscisco, CA, 3University of Pennsylvania, Philadlephia, PA

    Background/Purpose: The use of anti-PD-1 (aPD-1) immunotherapy has seen significant success in clinical practice, corresponding with a continued rise in clinical indications for multiple cancer…
  • Abstract Number: 1945 • ACR Convergence 2023

    Case Series of 6 Patients Exhibiting Myositis as a Rheumatologic Adverse Events Related to Cancer Immunotherapy in Two Spanish Hospitals

    Arturo Llobell1, Inigo Gonzalez-Mazon2, carmen secada3, Adrian Martin-Gutierrez3, Almudena García-Castaño3, Enrique Gallardo4, Soledad Retamozo5, Antonio Gomez-Centeno6, Luis Fernandez-Morales4, Jordi Gratacos Masmitja7 and Ricardo Blanco8, 1Parc Tauli University Hospital, Barcelona, Spain, 2Hospital Universitario Marques de Valdecilla, Santander, Spain, 3Hospital Universitario Marqués de Valdecilla, Santander, Spain, 4Parc Taulí University Hospital, Sabadell, Spain, 5Laboratory of Autoimmune Diseases Josep Font, IDIBAPS-CELLEX, Barcelona, Spain, 6Parc Taulí Hospital Universitari, Sabadell, Spain, 7University Hospital Parc Taulí, Sabadell, Spain, 8Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain

    Background/Purpose: Myositis is a rare inflammatory complication associated with immune related adverse events (irAE) of immune checkpoints inhibition (ICI) immunotherapy1. It is characterized by musculoskeletal…
  • Abstract Number: 129 • 2023 Pediatric Rheumatology Symposium

    Interrogation of STAT3 Activation in Patients with Polyarticular Juvenile Arthritis (polyJIA)

    Stephanie Wood1, Justin Branch1, Priscilla vasquez1, Marietta De Guzman1, Amanda Brown2, A. Carmela Sagcal-Gironella3, Saimun Singla4, Andrea Ramirez5 and Tiphanie Vogel5, 1Baylor College of Medicine, Texas Children's Hospital, Houston, TX, 2University of Arkansas for Medical Sciences, Little Rock, AR, 3Hackensack University Medical Center, Hackensack, NJ, 4Self, Houston, TX, 5Baylor College of Medicine, Houston, TX

    Background/Purpose: A better understanding of the pathogenesis of polyJIA is necessary to guide more effective clinical care, such as the development of data-driven approaches to…
  • Abstract Number: 020 • 2023 Pediatric Rheumatology Symposium

    Generation of Human Resident Memory T Cells in 3D Synovial Organoid Model

    Margaret Chang1, Maryrose Hahn1, Brian Wauford1, Rachel Blaustein2, Kevin Wei2 and Peter Nigrovic1, 1Boston Children's Hospital, Boston, MA, 2Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Most rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) patients experience episodic arthritis flares and require life-long medications to control their disease. We observed…
  • Abstract Number: L03 • ACR Convergence 2022

    A Phase 2 Trial of Peresolimab for Adults with Rheumatoid Arthritis

    Jay Tuttle1, Edit Drescher2, Jesus Abraham Simón-Campos3, Paul Emery4, Maria Greenwald5, Alan Kivitz6, Hyungmin Rha1, Pia Yachi1, Christina Kiley1 and Ajay Nirula7, 1Eli Lilly and Company, Indianapolis, IN, 2Csolnoky Ferenc Hospital, Veszprém, Hungary, 3Köhler & Milstein Research/Hospital Agustín O'Horán, Merida, Yucatan, Mexico, 4University of Leeds, Leeds, United Kingdom, 5Desert Medical Advances, Palm Desert, CA, 6Altoona Center for Clinical Research, Duncansville, PA, 7Eli Lilly, San Diego, CA

    Background/Purpose: Peresolimab is a humanized immunoglobulin G1 monoclonal antibody that stimulates human programmed cell death protein 1 (PD-1). We hypothesized that peresolimab binding to PD-1,…
  • Abstract Number: 0053 • ACR Convergence 2022

    Natural Microbial Exposure Increases Susceptibility of C57BL/6 Mice to Collagen-induced Arthritis

    Sahar Lotfi-Emran1 and David Masopust2, 1University of Minnesota, Minneapolis, MN, 2University of Minnesota, Department of Microbiology and Immunology, Minneapolis, MN

    Background/Purpose: Mice exposed to natural microbes (NME) develop an appropriately mature immune system, one that resembles that of a non-neonatal human.1,2 Collagen induced arthritis is…
  • Abstract Number: 0651 • ACR Convergence 2022

    Inflammatory Dendritic Cell Drive Intra-renal T Cells to Double-negative T Cell in Lupus Nephritis

    Latha Prabha Ganesan, Shane Bruckner, Noushin Saljoughian, James Turman, Murugesan Rajaram, Brad Rovin, Wael Jarjour and Samir Parikh, The Ohio State University, Columbus, OH

    Background/Purpose: The pathogenesis of lupus nephritis (LN) is incompletely understood stalling progress and resulting in suboptimal patient outcomes. We previously identified a novel inflammatory dendritic…
  • Abstract Number: 1702 • ACR Convergence 2022

    Targeting CD6-CD318 Axis with UMCD6 (anti-CD6) Enhances in Vivo Killing of Cancer Cells Through Direct Activation of NK Cells

    Mikel Gurrea-Rubio1, Qi Wu1, Eliza Pei-Suen Tsou1, M. Asif Amin1, Phillip Campbell1, Peggy Randon1, Matthew Lind1, Sarah Ory1, Camila Amarista1, Sirapa Vichaikul2, Jeffrey Ruth1, Feng Ling3 and David Fox1, 1University of Michigan, Ann Arbor, MI, 2Michigan Medicine, Howell, MI, 3Cleveland Clinic, Cleveland, OH

    Background/Purpose: Immune checkpoint inhibitors represent a major advance in cancer treatment, but disease prognosis continues to be poor for most patients. Resistance of cancer cells…
  • « Previous Page
  • 1
  • …
  • 14
  • 15
  • 16
  • 17
  • 18
  • …
  • 26
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

Embargo Policy

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM CT on October 25. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2026 American College of Rheumatology